Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g25130 | A05 | 30056594 | G | A | synonymous_variant | LOW | c.2103C>T|p.Phe701Phe |
S291 |
2 | BAA05g25130 | A05 | 30057310 | C | T | missense_variant | MODERATE | c.1387G>A|p.Ala463Thr |
S155 S211 |
3 | BAA05g25130 | A05 | 30058068 | G | A | missense_variant | MODERATE | c.629C>T|p.Pro210Leu |
S168 |
4 | BAA05g25130 | A05 | 30058072 | G | A | missense_variant | MODERATE | c.625C>T|p.Leu209Phe |
S187 |
5 | BAA05g25130 | A05 | 30059671 | C | T | upstream_gene_variant | MODIFIER | c.-196G>A| |
S140 |
6 | BAA05g25130 | A05 | 30061514 | G | A | upstream_gene_variant | MODIFIER | c.-2039C>T| |
S25 |
7 | BAA05g25130 | A05 | 30064087 | A | T | upstream_gene_variant | MODIFIER | c.-4612T>A| |
S308 |
8 | BAA05g25130 | A05 | 30064337 | C | T | upstream_gene_variant | MODIFIER | c.-4862G>A| |
S246 |
9 | BAA05g25130 | A05 | 30064348 | C | T | upstream_gene_variant | MODIFIER | c.-4873G>A| |
S33 |